Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion> ?p ?o ?g. }
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- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion type Assertion NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_head.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion description "[A wide spectrum of genetic aberrations has been associated with MDS, including chromosomal translocations involving the NUP98 gene, most commonly leading to fusions of NUP98 with abd-b group HOX genes, including HOXD13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion evidence source_evidence_literature NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion SIO_000772 18648006 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion wasDerivedFrom befree-20140225 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.
- NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_assertion wasGeneratedBy ECO_0000203 NP505231.RA_-Hr1T7I_0kwQPAMV8XT_PsIuXCz0az-5mmEGcdkMME130_provenance.